Augusto B. Silva
Feira De Santana, BA, Brazil
Last Updated: 09/26/2026
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Found 10 publications
Infrared spectroscopy as a new approach for early fabry disease screening: a pilot study.
Journal: Orphanet journal of rare diseases
Published: June 25, 2024
Assessment of combined α-GAL enzyme activity and lyso-GL3 for Fabry disease screening in women with chronic kidney disease.
Journal: Molecular genetics and metabolism
Published: May 17, 2024
Baseline characteristics and evolution of Brazilian patients with atypical hemolytic uremic syndrome: first report of the Brazilian aHUS Registry.
Journal: Clinical kidney journal
Published: January 24, 2022
Brazilian consensus recommendations for the diagnosis, screening, and treatment of individuals with fabry disease: Committee for Rare Diseases - Brazilian Society of Nephrology/2021.
Journal: Jornal brasileiro de nefrologia
Published: August 26, 2021
Recommendations for the diagnosis and management of Fabry disease in pediatric patients: a document from the Rare Diseases Committee of the Brazilian Society of Nephrology (Comdora-SBN).
Journal: Jornal brasileiro de nefrologia
Published: April 09, 2021
COMDORA-SBN recommendations for patients with rare kidney diseases in relation to the Covid-19 pandemic.
Journal: Jornal brasileiro de nefrologia
Published: September 03, 2020
Renal Manifestations of Fabry Disease: A Narrative Review.
Journal: Canadian journal of kidney health and disease
Published: May 26, 2020
Case report: is low α-Gal enzyme activity sufficient to establish the diagnosis of Fabry disease?
Journal: Jornal brasileiro de nefrologia
Published: October 18, 2016
Showing 1-10 of 10
Last Updated: 09/26/2026